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Computerised cognitive behavioural therapy (CBT) for common mental disorders

Computerised cognitive behavioural therapy (CBT) for common mental disorders: a randomised controlled trial (RCT) of a workplace intervention

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN24529487
Enrollment
535
Registered
2010-05-12
Start date
2009-06-26
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Topic: Mental Health Research Network

Interventions

MoodGYM is a modularised course, designed to last 6 weeks, which participants will follow at their own pace. Weekly, brief (10-minute) calls will be made to check on use of MoodGYM or other services (

Sponsors

The Institute of Mental Health (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. A positive response to any of the questions 1 - 3 of the Brief Patient Health Questionnaire (PHQ-Brief), indicating: 1.1. Major depression 1.2. Other depressive syndromes (2 - 5 symptoms more than half the days over 2 weeks affecting function at home, work or socially), or 1.3. Panic syndrome (at least one panic in the last 4 weeks affecting function at home, work or socially) Mood Gym is supposed to manage all these problems and any of them is likely to lead to problems at work. OR 2. On Patient Health Questionnaire-9 (PHQ-9), employee scores 2 or more on 5 of the 9 items including 2 on item 1 or 2 and "somewhat difficult" on item 10 (function). These scores are equivalent symptomatically to a diagnosis of major depression AND 3. Age over 18 years and under 65 years, either sex

Exclusion criteria

Exclusion criteria: 1. Has a primary alcohol or drug use problem 2. Depression secondary to organic brain disease, e.g., stroke 3. Bipolar disorder or other serious mental illness apart from unipolar depression 4. Is already receiving cognitive behaviour therapy 5. Has current suicide plans requiring emergency psychiatric treatment 6. Does not or cannot give written informed consent to the study

Design outcomes

Primary

MeasureTime frame
1. Patient Health Questionnaire (PHQ9) 2. Work Limitations Questionnaire, WLQ 3. Generalised Anxiety Disorder Assessment (GAD7) Measured at baseline, 6 weeks and 12 weeks.

Secondary

MeasureTime frame
1. Clinical Outcomes in Routine Evaluation (CORE10) 2. Work and Social Attitudes Scale (WSAS) Measured at baseline, 6 weeks and 12 weeks.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 8, 2026